Cited by 479Single-cell and spatial transcriptomicsCell Image Analysis TechniquesDevelopmental Biology and Gene Regulation

The DOI matches its Crossref record; 216 of the 219 references it cites were found in a registry or an index; none of the 60 sources its claims cite is checked for support yet.

What is a cell type and how to define it?

Open access
Zeng, Hongkui·2022·Cell

Abstract

Cell types are the basic functional units of an organism. They exhibit diverse phenotypic properties at multiple levels, making them challenging to define, categorize and understand. This Review provides an overview of the basic principles of cell types rooted in evolution and development, and discusses approaches to characterize and classify cell types and investigate how they contribute to the organism’s function, using the mammalian brain as a primary example. I propose a roadmap towards a conceptual framework and knowledge base of cell types that will enable a deeper understanding of the dynamic changes of cellular function under healthy and diseased conditions.

Overview

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Written from the paper’s full text.

TL;DR

This review argues that cell types arise through evolution and have identities encoded in the genome, and it proposes a multilevel, iterative roadmap anchored in single-cell transcriptomic taxonomy and refined by epigenomic, spatial, anatomical, physiological, functional, developmental, and cross-species evidence. It illustrates these ideas mainly with the mammalian brain, especially mouse cortex.

Key findings

  • Single-cell transcriptomic taxonomies in adult mammalian brain are consistently hierarchical: neuronal versus non-neuronal classes at the top, then major brain structures/regions, then subclasses and types; in mouse cortex, glutamatergic neurons divide into nine subclasses and GABAergic neurons into six, giving about 110 transcriptomic types per cortical area.
  • Transcriptomic types correspond well with spatial organization and some multimodal properties: mouse retina studies converge on roughly 130 neuron types, cortical transcriptomic continua align with laminar depth, and Patch-seq/MERFISH link transcriptomic variation to morphology, electrophysiology, and layer position.
  • Cell types must be distinguished from cell states; transcriptomic snapshots can mix transient states with stable identities, and non-neuronal cells such as astrocytes, oligodendrocytes, microglia, and vascular cells show pronounced state changes across development, aging, injury, and disease.
  • The proposed roadmap is to use transcriptomic taxonomy as an anchor, add epigenomic and spatial transcriptomic data, integrate anatomy, physiology, connectivity, and function with molecular identification, study development and cross-species evolution, and organize results in a branching, tree-like classification with standardized ontology and nomenclature.

Methods

  • Design: conceptual review and synthesis, not a primary empirical study; no new sample or dataset is reported.
  • Evidence base: literature on cell-type characterization across molecular, morphological, physiological, functional, developmental, and evolutionary modalities, with the mammalian brain and mouse cortex as main examples.
  • Analysis: narrative integration of single-cell transcriptomics, epigenomics, spatially resolved transcriptomics, Patch-seq, connectomics, lineage/trajectory studies, and cross-species comparisons; concludes with a proposed roadmap.

Limitations

  • The paper states that no consistent standard definition of cell types exists; it is often unclear whether types defined by different phenotypic features agree, and transcriptomic clusters at the lowest hierarchical levels have not been fully validated.
  • It notes technical and conceptual gaps: continuous variation makes exact type counts difficult; cross-species comparisons need well-annotated genomes, comparable ontologies, and high-quality data; single-cell proteomics and mammalian connectomics remain under development; links between transcriptomic types and projection or functional properties are unresolved.
  • Evident from the text: as a review, it presents no new experimental tests of its roadmap, and its examples are heavily weighted toward mammalian brain and mouse cortex, so generality to other organs and species is asserted rather than demonstrated.

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Integrity signals

Registry

Crossref · 10.1016/j.cell.2022.06.031

Cites

216 of 216 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

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Show all 27 claims

  • It may state two separate claims as one. 15
  • Probably not a substantial claim. 17
27 of 27
  • The paper relies on this without support.

    Cell types are the basic functional units of an organism.

    “Cell types are the basic functional units of an organism.”
  • The paper relies on this without support.

    There has not been a consistent and standard definition of cell types.

    “However, there has not been a consistent and standard definition of cell types even though it is critical for reproducible investigation.”
  • The paper relies on this without support.

    It is often unclear whether cell types defined by different phenotypic features agree, nor which feature is the right one to define cell types.

    “It is often unclear if cell types defined by different phenotypic features agree with each other, nor which feature is the “right” one to define cell types.”
  • The paper relies on this without support.

    Cellular properties at individual cell level are highly heterogeneous, and variations in different modalities do not necessarily exhibit high concordance, making it often impossible to define exactly what is a cell type and draw clear boundaries between types.

    “At the same time, cellular properties at individual cell level are highly heterogeneous, variations in different modalities do not necessarily exhibit high degrees of concordance, making it often impossible to define exactly what is a cell type and draw clear boundaries between “types”.”
  • The paper relies on this without support.

    The vast majority of cortical and subcortical neuron types have long-range axon projections forming circuit networks throughout the brain.

    “The vast majority of cortical and subcortical neuron types have long-range axon projections to form circuit networks throughout the brain.”
  • The paper relies on this without support.

    Transcriptomes are rich in containing molecular correlates of all sorts of cellular properties.

    “Since transcriptomes are rich in containing the molecular correlates of all sorts of cellular properties”
  • The paper relies on this without support.

    Emergence of a new cell type during development is more often the consequence of cell division from which a daughter cell takes up a new cell type identity.

    “More often, emergence of a new cell type during development is the consequence of cell division from which a daughter cell takes up a new cell type identity (Fig. 4).”
  • The paper relies on this without support.

    Coordinated neuronal activities in brain circuits generate sensory perception and behavior.

    “Coordinated neuronal activities in brain circuits generate sensory perception and behavior.”
  • The paper relies on this without support.

    IEG activation leads to expression of downstream effectors, such as ion channels or synaptic proteins, that shape cell states and remodel neuronal connections.

    “IEG activation leads to expression of downstream effectors, such as ion channels or synaptic proteins, that shape the cell states and remodel neuronal connections.”
  • The paper relies on this without support.

    Cell state changes in the brain are closely related to neural plasticity.

    “Cell state changes in the brain are closely related to neural plasticity.”
  • The paper relies on this without support.

    Various diseased conditions can induce pathological changes in cell states in different brain regions or tissue organs.

    “Similarly, various diseased conditions can induce pathological changes in cell states in different brain regions or tissue organs.”
  • The paper relies on this without support.

    Numerous studies have revealed selective vulnerability of specific cell types for specific diseases.

    “Numerous studies have revealed selective vulnerability of specific cell types for specific diseases.”
  • The paper relies on this without support.

    Astrocytes become reactive under pathological conditions.

    “Astrocytes become reactive under pathological conditions.”
  • The paper relies on this without support.

    Oligodendrocytes are the myelinating cells of the CNS generated from OPCs throughout life.

    “Oligodendrocytes are the myelinating cells of the central nervous system (CNS) that are generated from OPCs throughout life.”
  • The paper relies on this without support.

    Microglia are the primary innate immune cells in the CNS and have a distinct developmental origin from peripheral immune cells.

    “Finally, microglia are the primary innate immune cells in the CNS and have a distinct developmental origin from peripheral immune cells.”
  • The paper relies on this without support.

    Microglia are generated from mesodermal progenitors that arise from the yolk sac and are among the earliest residential cell types in the brain.

    “They are generated from mesodermal progenitors that arise from the yolk sac and are among the earliest residential cell types in the brain.”
  • The paper relies on this without support.

    Microglia can be both responders to and inducers of various neurodegenerative, neuroinflammatory and neurodevelopmental diseases.

    “In particular, microglia can be both responders to and inducers of various neurodegenerative, neuroinflammatory and neurodevelopmental diseases.”
  • The paper relies on this without support.

    The entire repertoire of cell types is built through sequential and parallel developmental events starting from the zygote.

    “The entire repertoire of cell types in the brain and the body is built through a sequential and parallel series of spatially and temporally coordinated developmental events starting from a single fertilized egg, the zygote.”
  • The paper relies on this without support.

    Transcriptional and epigenetic regulatory programs are unfolded from genome sequences and drive proliferation and differentiation leading to diverse cellular phenotypes.

    “Transcriptional and epigenetic regulatory programs are unfolded from the genome sequences and drive a cascading series of cell proliferation and differentiation processes leading to the manifestation of diverse cellular phenotypes.”
  • The paper relies on this without support.

    Earlier-stage ancestral cell types are fewer and more multipotent, giving rise to more descendant cell types with increasingly restricted fates.

    “In the developmental ontogeny of cell types, earlier-stage ancestral cell types are fewer and are more multipotent, they give rise to a larger number of descendant cell types with increasingly restricted fates.”
  • The paper relies on this without support.

    The developmental program specifies a spatial plan, including the location of organs and the spatial organization of cell types.

    “The developmental program rolls out not only a temporal but also an elaborate spatial plan, specifying the location of each tissue organ and the spatial organization of all the cell types within each.”
  • The paper relies on this without support.

    Brain development includes patterning and regionalization, neurogenesis and neuronal migration, gliogenesis and glia differentiation, neuronal differentiation and circuit formation, and circuit refinement and plasticity.

    “For the brain, the main series of events of brain development leading to the mature adult-stage cell types and circuits include: patterning and regionalization (laying out the master plan of brain architecture), neurogenesis and neuronal migration, gliogenesis and glia cell differentiation, neuronal differentiation and circuit formation (axonogenesis, dendritic arborization, synaptogenesis, myelin”
  • The authors state this as an assumption.

    Transcriptomic changes tend to be more continuous during cell state transitions and more abrupt or discrete when cells switch their types.

    “Although not absolute, it is reasonable to assume that transcriptomic changes tend to be more continuous during cell state transitions, and more abrupt or discrete when cells switch their types.”
  • The paper relies on this without support.

    A neuron type usually has multiple projection targets and individual neurons can choose a subset specifically or randomly.

    “Since a neuron type usually has multiple projection targets and a neuron within that type can choose a subset of those targets either specifically or randomly”
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Metadata

Authors
Zeng, H.
Affiliations
Allen Institute for Brain Science (US)
Corresponding author
Zeng, Hongkui
Venue
Cell
Publisher
Elsevier BV
Published
2022-07
Volume
185
Issue
15
Pages
2739-2755
ISSN
0092-8674 (ISSN-L)
OpenAlex
W4286449197
Cited by
439
References
219
Citations by year
2026: 95 · 2025: 126 · 2024: 121 · 2023: 83 · 2022: 13
FWCI
8.98
Type
journal article
Language
en
Open access
Locations
  • Cell (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • NIMH (U19MH114830)
  • National Institutes of Health
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Cell Image Analysis Techniques
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
cell types, cell type classification, mammalian brain, cell function, cellular heterogeneity
MeSH terms
Animals, Brain, Humans, Mammals, Single-Cell Analysis

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